Las Vegas, Nevada
Clinical Research Coordinator Job Opening in Las Vegas, Nevada - Clinical Research Coordinator JOB FUNCTION:
The primary function of the Clinical Research Coordinator is to coordinate and conduct clinical research in the in-hospital and clinic settings with an emphasis on the screening, enrollment, and monitoring of patient
*REPORTS TO: *
SENIOR DIRECTOR CLINICAL OPERATIONS
*PRINCIPAL DUTIES AND RESPONSIBILITIES: *
* Serves as primary study coordinator for research protocols at affiliated hospitals or in the outpatient clinic setting as assigned by Director.
* Directs the conduct of clinical studies to ensure adherence to the research protocol and provides bimonthly updates to Principal Investigator on study progress.
* Screens patient records, databases, and physician referral summaries for identification of prospective candidates for research protocols.
* Interviews prospective subjects for participation in investigations and obtains informed consent.
* Participates in initiation visits/investigator?s meetings for assigned clinical trials (may involve travel) and implements these trials according to a deadline schedule mutually agreed upon by PI and sponsor.
* Develops study working folders for assigned protocols to outline guidelines for protocol compliance and to assure complete source documentation.
* Educates human subjects for participation in investigations.
* Educates clinic/hospital personnel for participation in protocol conduct, data collection process, and related conceptual issues as applicable.
* Maintains consistent enrollment in protocols and provides weekly written documentation of activities.
* Coordinates the collection of data according to the research protocol, operations manual, and case report form guidelines within the budgetary guidelines established by Director.
* Draws, prepares, and ships laboratory samples for clinical trials.
* Maintains investigational drug/device dispensing accountability and shipping logs according to protocol guidelines.
* Performs EKGs, and other procedures as directed by study protocol
* Instructs Principal Investigator on procedures and tests that need to be performed in compliance with the study protocol and advises Principal Investigator on the results of procedures and tests; calling to attention findings of clinical importance.
* Documents research related examinations, procedures, tests, and other activities in appropriate clinic or hospital charts.
* Completes phone logs for conversations with sponsors, patients, physicians, and coordinating organizations.
* Schedules follow-up visits for study patients in collaboration with Principal Investigator and provides source documentation for the activities conducted during these visits.
* Completes accurate and complete data entry into case report forms or pre-established computer programmed formats ensuring appropriate source documentation.
* Schedules and undergoes sponsor initiated monitor visits and quality assurance audits for periodic reviewing and querying of collected data in a timely fashion.
* Identifies strategies to improve patient enrollment in research protocols in collaboration with Principal Investigator.
* May perform other duties not specifically listed in this job description as assigned by their immediate supervisor
QUALIFICATIONS:
* Associate?s Degree in a Healthcare or Clinical Research related field required; Bachelor?s Degree in a Healthcare or Clinical Research related field preferred;
* Minimum of two (2) years of research experience.
* Certified Clinical Research Coordinator (CCRC) or Certified Clinical Research Associate (CCRA), preferred;
* Proficient in word processing, computer spreadsheets, mainframe computer applications, and database management.
* Ability to prioritize and organize a high volume workload and changing priorities.
* Familiar with principles of protocol development, study design, statistics, and IRB process.
* Valid driver's license and reliable transportation required.
The above information on this portion is designed to present the most essential duties and responsibilities necessary to achieve the positions end results. The occupant of this position is required to follow any other job-related instructions and perform any other duties as requested by Physician Director(s), Clinical Research Manager, and/or Practice Manager. It is the responsibility of each employee to assist other office staff when and where necessary. All employees have the responsibility of answering phones, maintaining files, filing, and updating data, etc. Most importantly, it is each staff member?s responsibility to project and maintain a positive attitude toward all patients and fellow coworkers. The duties listed may be changed or modified at any time.
Job Type: Full-time
Required education:
Bachelor's
Required experience:
Clinical Research: 2 years
Phlebotomy: 1 year
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